硫化氢抑制糖酵解调控小胶质细胞 对帕金森抑郁保护机制的研究
摘要
转化,从而改善帕金森病抑郁的作用机制。方法:将培养的BV2小胶质细胞随机分为4组:对照组(Sham组)、脂
多糖组(LPS组)、LPS+硫氢化钠组(NaHS组)、LPS+生理盐水组(NS组)。选取60只SPF级大鼠,随机分为对照
组(Sham组)、PD+皮质酮组(模型组)、PD+皮质酮+NaHS(NaHS组)、PD+皮质酮+NS(NS组),每组5-10
只,其中对照组15只,其余45只用于建立帕金森病合并抑郁大鼠模型。NS组注射生理盐水,NaHS组注射NaHS。
通过Western-blot检测各组PDC、PDK2的表达水平,用乳酸试剂盒测定乳酸浓度,采用免疫荧光技术分析CD68
的表达水平,并利用RT-qPCR技术检测小胶质细胞炎症因子肿瘤坏死因子-α(TNF-α)、诱导型一氧化氮合
酶(iNOS)及白细胞介素-10(IL-10)的释放情况。动物实验中,通过旷场实验和高架十字迷宫来检测NaHS对帕
金森病合并抑郁的影响。结果:体外实验结果表明,与LPS组和NS组相比,NaHS组显著降低了PDK2的表达,同
时提高了PDC的表达,并减少乳酸浓度;此外,NaHS组的CD68平均荧光强度低于LPS组和NS组,且该组细胞中
iNOS、TNF-α水平下降,IL-10水平上升。动物实验结果显示,与模型组相比,NaHS组组织中的iNOS、TNF-α
水平降低,而IL-10水平升高。在旷场实验中,NaHS组小鼠进入中心区域的次数和停留时间均增加;十字迷宫实验
结果表明,NaHS组小鼠在开放区域的进入次数和停留时间也有所增加。结论:H2S通过抑制糖酵解促进小胶质细胞
向M2型极化,从而缓解帕金森病合并抑郁的症状。
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